510(k) K945124 ยท GDF Guide, Needle, Surgical
BREAST LESION LOCALIZATION NEEDLE
| Applicant | Promex, Inc., Indianapolis IN, US |
| Decision | Substantially Equivalent, Nov 22, 1994 |
| Received | Oct 19, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K945124
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.